Ravdin P M, Berg D K
Proc Natl Acad Sci U S A. 1979 Apr;76(4):2072-6. doi: 10.1073/pnas.76.4.2072.
Bungarus multicinctus venom contains several alpha-toxins in addition to the widely used alpha-bungarotoxin (Bgt 2.2). We have found that two of the alpha-toxins (Bgt 3.1 and 3.3) inhibit neuronal acetylcholine (AcCho) sensitivity when tested on ciliary ganglion neurons in cell culture. Over 90% of the AcCho sensitivity recorded in response to iontophoretic application of AcCho was blocked when the neurons were incubated with either of the toxins at 10(-7) M for 1 hr at 37 degrees C. The blockade could be partially reversed by incubating the neurons for 1-2 hr in medium lacking the toxins. The neurons also had a high-affinity binding site for Bgt 2.2, as indicated by binding studies with rhodamine-labeled Bgt 2.2. Concentrations of Bgt 2.2(10(-7) M) that should be nearly adequate to saturate the high-affinity site, however, had no detectable effect on AcCho sensitivity of the neurons. Higher concentrations of Bgt 2.2(10(-5) M) produced a partial inhibition of AcCho sensitivity, suggesting either that the neurons had two classes of binding sites for Bgt 2.2 (with the low-affinity site affecting AcCho sensitivity) or that the preparation of Bgt 2.2 contained minor components (e.g., Bgt 3.1 or 3.3) that were responsible for the blockade. The mechanisms by which Bgt 3.1 and 3.3 inhibit neuronal AcCho sensitivity remain unknown. If they bind specifically to the AcCho receptor, they will be useful agents for studying the distribution and regulation of this membrane component.
除了广泛使用的α-银环蛇毒素(Bgt 2.2)外,多环眼镜蛇毒还含有几种α-毒素。我们发现,在细胞培养中对睫状神经节神经元进行测试时,其中两种α-毒素(Bgt 3.1和3.3)会抑制神经元对乙酰胆碱(AcCho)的敏感性。当神经元在37℃下与10⁻⁷M的任何一种毒素孵育1小时后,通过离子电泳施加AcCho所记录到的超过90%的AcCho敏感性被阻断。将神经元在不含毒素的培养基中孵育1 - 2小时,这种阻断作用可部分逆转。结合研究表明,用罗丹明标记的Bgt 2.2进行研究时,神经元对Bgt 2.2也有高亲和力结合位点。然而,理论上几乎足以饱和高亲和力位点的Bgt 2.2浓度(10⁻⁷M)对神经元的AcCho敏感性没有可检测到的影响。较高浓度的Bgt 2.2(10⁻⁵M)对AcCho敏感性产生了部分抑制作用,这表明要么神经元对Bgt 2.2有两类结合位点(低亲和力位点影响AcCho敏感性),要么Bgt 2.2制剂中含有导致阻断作用的次要成分(例如Bgt 3.1或3.3)。Bgt 3.1和3.3抑制神经元AcCho敏感性的机制尚不清楚。如果它们特异性结合到AcCho受体上,将成为研究这种膜成分分布和调节的有用试剂。